Pascal Laforêt

15.4k total citations
270 papers, 7.4k citations indexed

About

Pascal Laforêt is a scholar working on Molecular Biology, Physiology and Rheumatology. According to data from OpenAlex, Pascal Laforêt has authored 270 papers receiving a total of 7.4k indexed citations (citations by other indexed papers that have themselves been cited), including 118 papers in Molecular Biology, 100 papers in Physiology and 93 papers in Rheumatology. Recurrent topics in Pascal Laforêt's work include Glycogen Storage Diseases and Myoclonus (90 papers), Lysosomal Storage Disorders Research (78 papers) and Mitochondrial Function and Pathology (50 papers). Pascal Laforêt is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (90 papers), Lysosomal Storage Disorders Research (78 papers) and Mitochondrial Function and Pathology (50 papers). Pascal Laforêt collaborates with scholars based in France, Netherlands and United States. Pascal Laforêt's co-authors include B. Eymard, Anthony Béhin, Michel Fardeau, Tanya Stojkovic, Karim Wahbi, B. Eymard, Norma B. Romero, Denis Duboc, Anne Lombès and Damien Sternberg and has published in prestigious journals such as The Lancet, JAMA and Nature Genetics.

In The Last Decade

Pascal Laforêt

251 papers receiving 7.2k citations

Peers

Countries citing papers authored by Pascal Laforêt

Since Specialization

Citations

This map shows the geographic impact of Pascal Laforêt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Pascal Laforêt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pascal Laforêt more than expected).

Fields of papers citing papers by Pascal Laforêt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pascal Laforêt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Pascal Laforêt. The network helps show where Pascal Laforêt may publish in the future.

Co-authorship network of co-authors of Pascal Laforêt

This figure shows the co-authorship network connecting the top 25 collaborators of Pascal Laforêt. A scholar is included among the top collaborators of Pascal Laforêt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pascal Laforêt. Pascal Laforêt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure 2025 ·Revue Neurologique ·Diana Maria Chiţimuș, Clovis Adam, Cécile Cauquil, Boris Keren, Nicholas Heming, (unknown), Djillali Annane, Guillaume Nicolas, Pascal Laforêt, Corinne Métay, (unknown)	0
2	Clinical insights in enzyme replacement therapy for metabolic storage disorders: lessons from Pompe disease 2025 ·The Lancet Neurology ·Nadine A. M. E. van der Beek, (unknown), Johanna M. P. van den Hout, W.W.M. Pim Pijnappel, Benedikt Schoser, Pascal Laforêt, Giancarlo Parenti, Pieter A. van Doorn, Ans T. van der Ploeg	2
3	Improving outcome measures in late onset Pompe disease: Modified Rasch‐Built Pompe‐Specific Activity scale 2024 ·European Journal of Neurology ·(unknown), Mike Horton, Stephan Wenninger, Haris Babačić, Benedikt Schoser, (unknown), (unknown), Pascal Laforêt, Sonia Segovia, Jordi Díaz‐Manera, Kristl G. Claeys, Tiziana Mongini, Olimpia Musumeci, (unknown), Thomas Hundsberger, Esther Brusse, Pieter A. van Doorn, Ans T. van der Ploeg, Nadine A. M. E. van der Beek	1
4	Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort 2023 ·European Journal of Neurology ·(unknown), (unknown), (unknown), Stéphane Vassilopoulos, Anthony Béhin, Céline Tard, Maud Michaud, (unknown), Savine Vicart, Marion Masingue, Robert‐Yves Carlier, Norma B. Romero, Emmanuelle Lacène, France Leturcq, B. Eymard, Pascal Laforêt, Tanya Stojkovic	4
5	Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group 2021 ·Neuromuscular Disorders ·Alejandro Lucía, Andrea Martinuzzi, Gisela Nogales‐Gadea, Rosaline C. M. Quinlivan, (unknown), Deeksha Bali, Richard Godfrey, Ronald G. Haller, Priya S. Kishnani, Pascal Laforêt, Nicoline Løkken, Olimpia Musumeci, Alfredo Santalla, Mark A. Tarnopolsky, (unknown), John Vissing, Nicol C. Voermans, (unknown)	30
6	A Proteomics-Based Analysis Reveals Predictive Biological Patterns in Fabry Disease 2020 ·Journal of Clinical Medicine ·Abdellah Tebani, Wladimir Mauhin, Lénaïg Abily-Donval, Céline Lesueur, (unknown), Yann Nadjar, Juliette Berger, (unknown), Foudil Lamari, Pascal Laforêt, Esther Noël, Stéphane Marret, Olivier Lidove, Soumeya Bekri	32
7	Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy 2019 ·Medicine ·Abdallah Fayssoil, Tanya Stojkovic, Adam Ogna, Pascal Laforêt, Hélène Prigent, Frédéric Lofaso, David Orlikowski, Guillaume Bassez, B. Eymard, Anthony Béhin	3
8	Effects of Home Mechanical Ventilation on Left Ventricular Function in Sarcoglycanopathies (Limb Girdle Muscular Dystrophies) 2018 ·The American Journal of Cardiology ·Abdallah Fayssoil, Lee S. Nguyen, Adam Ogna, (unknown), Olivier Nardi, Pascal Laforêt, Bernard Clair, Hélène Prigent, Frédéric Lofaso, France Leturcq, Rabah Ben Yaou, Djillali Annane, David Orlikowski	2
9	Genetic Mutations and Demographic, Clinical, and Morphological Aspects of Myofibrillar Myopathy in a French Cohort 2018 ·Genetic Testing and Molecular Biomarkers ·Alzira Alves de Siqueira Carvalho, (unknown), Guy Brochier, (unknown), (unknown), (unknown), (unknown), Konstantinos Papadopoulos, Anthony Béhin, Pascal Laforêt, T. Stojkovic, B. Eymard, Michel Fardeau, Norma B. Romero	16
10	Diaphragm: Pathophysiology and Ultrasound Imaging in Neuromuscular Disorders 2017 ·Journal of Neuromuscular Diseases ·Abdallah Fayssoil, Anthony Béhin, Adam Ogna, D. Mompoint, Helge Amthor, Bernard Clair, Pascal Laforêt, Arnaud Mansart, Hélène Prigent, David Orlikowski, Tanya Stojkovic, Stéphane Vinit, Robert Carlier, B. Eymard, Frédéric Lofaso, Djillali Annane	76
11	Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa 2017 ·Molecular Genetics and Metabolism ·V. Decostre, Pascal Laforêt, Marie De Antonio, (unknown), Aurélie Canal, G. Ollivier, Aleksandra Nadaj‐Pakleza, François Petit, Karim Wahbi, Abdallah Fayssoil, B. Eymard, Anthony Béhin, Philippe Labrune, Jean‐Yves Hogrel	13
12	Phase 1 Safety and Pharmacokinetics of the Novel Enzyme Replacement Therapy neoGAA in Treatment-Naïve and Alglucosidase Alfa-Treated Late-Onset Pompe Disease Patients (S38.005) 2016 ·Neurology ·Jaya Trivedi, Ans van der Ploeg, Richard J. Barohn, Barry J. Byrne, Claude Desnuelle, Özlem Göker-Alpan, Shafeeq Ladha, Pascal Laforêt, Eugen Mengel, Alan Pestronk, Jean Pouget, Benedikt Schoser, Volker Straub, Philip Van Damme, John Vissing, Peter Young, Raheel Shafi, Kerry Culm-Merdek, (unknown), (unknown)	1
13	Multidisciplinary care allowing uneventful vaginal delivery in a woman with Pompe disease 2016 ·Neuromuscular Disorders ·Barbara Perniconi, Danièle Vauthier‐Brouzes, Capucine Morélot-Panzini, Marc Dommergues, J. Nizard, Nadjib Taouagh, Jean‐Yves Hogrel, Aurélie Canal, Laurent Servais, Pascal Laforêt	6
14	Minutes of the European POmpe Consortium (EPOC) Meeting March 27 to 28, 2015, Munich, Germany. 2015 ·PubMed ·Benedikt Schoser, Pascal Laforêt, (unknown), António Toscano, (unknown), (unknown)	4
15	Attitudes and expectations of patients with neuromuscular diseases about their participation in a clinical trial 2013 ·Revue Neurologique ·Marcela Gargiulo, (unknown), (unknown), Jean‐Yves Hogrel, Valérie Doppler, (unknown), S. Herson, (unknown), B. Eymard, Pascal Laforêt	3
16	Variable phenotype of del45-55 Becker patients correlated with nNOSµ mislocalization and RYR1 hypernitrosylation 2012 ·Human Molecular Genetics ·Christel Gentil, France Leturcq, Rabah Ben Yaou, Jean‐Claude Kaplan, Pascal Laforêt, I. Pénisson-Besnier, Caroline Espil‐Taris, Thomas Voït, Luis Garcı́a, France Piétri‐Rouxel	39
17	Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa 2012 ·Molecular Genetics and Metabolism ·Ans T. van der Ploeg, Richard J. Barohn, Lisa Carlson, Joel Charrow, Paula R. Clemens, Robert J. Hopkin, Priya S. Kishnani, Pascal Laforêt, Claire Morgan, Sharon Nations, Alan Pestronk, Horacio Plotkin, Barry E. Rosenbloom, Katherine B. Sims, Elisa Tsao	85
18	Juvenile-onset permanent weakness in muscle phosphofructokinase deficiency 2012 ·Journal of the Neurological Sciences ·Edoardo Malfatti, Nazha Birouk, Norma B. Romero, Monique Piraud, François Petit, Jean‐Yves Hogrel, Pascal Laforêt	11
19	Impact of late-onset Pompe disease on participation in daily life activities: Evaluation of the Rotterdam Handicap Scale 2007 ·Neuromuscular Disorders ·M.L.C. Hagemans, Pascal Laforêt, Wim Hop, Ingemar S. J. Merkies, Pieter A. van Doorn, A. J. J. Reuser, Ans T. van der Ploeg	40
20	AB26-1 2006 ·Heart Rhythm ·Frédéric Anselme, (unknown), Jop H. van Berlo, Gisèle Bonne, Arnaud Savouré, Rabah Ben Yaou, J. Peter van Tintelen, Henri-Marc Bécane, Maarten P. van den Berg, Pascal Laforêt, Alain Cribier, (unknown), Denis Duboc	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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